反応式
S(=O)(=O)(O)O.[CH3:6][CH:7]([CH2:11][CH2:12][CH2:13][CH:14]([CH3:16])[CH3:15])[CH2:8][CH2:9]O.[BrH:17]>>[CH3:6][CH:7]([CH2:11][CH2:12][CH2:13][CH:14]([CH3:16])[CH3:15])[CH2:8][CH2:9][Br:17]参加物
4
実験手順
48% HBr (200 ml) and concentrated sulfuric acid (0.46 ml) were added to 3,7-dimethyl-1-octanol (21.0 g, 157.9 mmol), and the mixture was heated overnight. After allowing to cool to room temperature, and the mixture was extracted with hexane. The organic layer was washed with 5% aqueous sodium hydrogen carbonate solution and saturated brine, dried and concentrated to give the title compound (28.7 g, 82.1%).
後処理
- temperaturethe mixture was heated overnight
- extractionthe mixture was extracted with hexane
- washThe organic layer was washed with 5% aqueous sodium hydrogen carbonate solution and saturated brine
- customdried
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-68ffd444f96c4333a3dda341ab53f8fc
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08846885B2
関連ノート
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